Abstract

We present a scaling model based on a moving boundary picture to describe heterogeneous gelation dynamics. The dynamics of gelation induced by different gelation mechanisms is expressed by the scaled equation for the time taken for development of the gel layer with a few kinetic coefficients characterizing the system. The physical meaning obtained by the analysis for a simple boundary condition from the standpoint of the phase transition shows that the time development of the gelation layer depends on whether the dynamics of the order parameter expressing the gelation of the polymer solution is fast or slow compared with the diffusion of the gelators in the heterogeneous gelation. The analytical method is used to understand the coagulation of blood from various animals. An experiment using systems with plasma coagulation occurring at interfaces with calcium chloride solution and with packed erythrocytes is performed to provide the data for model fitting and it is clarified that a few key kinetic coefficients in plasma coagulation can be estimated from the analysis of gelation dynamics.

Highlights

  • Used gels are prepared using chemical reagents while mixing, by lowering the temperature and by the irradiation of high-energy electromagnetic waves, such as an electron beam and UV, where the cross-linking sites of polymer networks are dispersed randomly in gels, resulting in a macroscopically isotropic and homogeneous structure

  • We show an illustration of one of the simplest cases, the one-dimensional growth of a gel in a polymer solution cell in contact with a gelator solution bath. This model was proposed for the analysis of gelation dynamics of chitosan solution induced by a change of pH

  • The gelation dynamics induced by the contact of polymer and gelator solutions was classified into several types and expressed by a system-independent scaling equation and system-dependent coefficients

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Summary

Introduction

Used gels are prepared using chemical reagents while mixing, by lowering the temperature and by the irradiation of high-energy electromagnetic waves, such as an electron beam and UV, where the cross-linking sites of polymer networks are dispersed randomly in gels, resulting in a macroscopically isotropic and homogeneous structure. Thiele and coworkers prepared anisotropic channel-like alginate gels induced by diffusion of various multivalent cations [5]. These are among the first examples of heterogeneous gelation, on which many studies have been reported [6,7,8,9,10,11,12,13,14,15,16,17].

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